Table 3.
PDE5 inhibitors oral single dose in clinical trials.
Drugs | Doses | Field | Phase | Patients | References and ID clinical number |
---|---|---|---|---|---|
Sildenafil | 100 mg | cognition | Completed Phase VI | Healthy males | Grass et al. 2001 [97] |
Sildenafil | 100 mg | cognition | Completed Phase VI | Healthy males | Schultheiss et al. 2001 [98] |
Sildenafil | 50 and 100 mg | schizophrenia | Completed Phase VI | Schizophrenic patients | Goff et al. 2009 [99] |
Sildenafil | 50 mg | Parkinson’s disease | Phase II (insufficient participants) | Parkinson’s disease patients | Identifier: NCT02162979 |
Sildenafil | 50 mg | hemodynamic function | N/A | AD patients | Sheg et al. 2017 [101] |
Sildenafil | ischemic stroke | Phase I (terminated due to non-recruitment of patients within the scheduled time period) | Ischemic stroke patients | Identifier: NCT00452582 | |
Tadalafil | 20 mg | cognition | Phase II | Elderly with small vessel disease | Identifier: NCT02450253 |
Vardenafil | 10, 20 mg | sensory gating | Completed phase II | Healthy young adults | Reneerkens et al 2013 [105] |
Vardenafil | 10, 20 mg | cognition | Completed phase II | Healthy young adults | Reneerkens et al 2013 [106] |
Udenafil | 100 mg | cognition | N/A | Patients with ED | Shim et al 2011 [102] |
Udenafil | 50 mg | cognition | N/A | Patients with ED | Shim et al. 2014 [103] |